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Campo Dublin Core | Valor | Idioma |
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dc.contributor.author | Vieira, Flaviana Tavares | - |
dc.contributor.author | Maia, José Roberto da Silveira | - |
dc.contributor.author | Vilela, Marcelo José | - |
dc.contributor.author | Ardisson, José Domingos | - |
dc.contributor.author | Santos, Marcelo Henrique dos | - |
dc.contributor.author | Oliveira, Tânia Toledo de | - |
dc.contributor.author | Nagem, Tanus Jorge | - |
dc.date.accessioned | 2017-06-19T14:32:55Z | - |
dc.date.available | 2017-06-19T14:32:55Z | - |
dc.date.issued | 2009 | - |
dc.identifier.citation | VIEIRA, F. T. et al. Spectroscopic investigation of organotin (IV) derivatives of 7-epiclusianone: a preliminary in vitro antitumor evaluation of HN-5 human carcinoma cell. Main Group Metal Chemistry, v. 32, p. 235-246, 2009. Disponível em: <https://www.degruyter.com/view/j/mgmc.2009.32.5/mgmc.2009.32.5.235/mgmc.2009.32.5.235.xml>. Acesso em: 20 mai. 2017. | pt_BR |
dc.identifier.issn | 2191-0219 | - |
dc.identifier.uri | http://www.repositorio.ufop.br/handle/123456789/7981 | - |
dc.description.abstract | A series of organotin(IV) compounds have been prepared by reaction with 7-epiclusianone (Epi), a natural product extracted from fruits of Rheedia gardneriana. This compound has an interesting motif with several coordinating sites for metal-ligand bond formation, and in solution, it shows a keto-enol tautomerism. The NMR of the organotin(IV) derivatives has revealed intramolecular hydrogen bonding, indicating that the keto-enol tautomerism of 7-epiclusianone is not involved upon coordination of those, but the absence of this bonding type in the case of the SnCl4 derivative suggests a strong interaction. The Mössbauer spectroscopy has revealed five- and six-fold coordination for the organotin(IV) and SnCL» derivatives in the solid state. However, in solution all tin complexes have six-fold coordination, as shown by "9Sn NMR. The overall data point out that the organotin(IV) precursors SnClxPri4_x (x = 1, 2) are weakly bonded to the 7- epiclusianone, except the SnC^. Bioassay in vitro of the substance test [SnClPh3(£/7/)] (1) has been investigated using two epithelial cells: normal MDCK from canine kidney, and IIN-5 from a human carcinoma of the tongue. The results clearly demonstrate that the time for cellular reproduction has been reduced in the presence of the substance test. | pt_BR |
dc.language.iso | en_US | pt_BR |
dc.rights | restrito | pt_BR |
dc.subject | 7-epiclusianone | pt_BR |
dc.subject | Organotin | pt_BR |
dc.subject | Carcinoma | pt_BR |
dc.subject | Spectroscopy | pt_BR |
dc.title | Spectroscopic investigation of organotin (IV) derivatives of 7-epiclusianone : a preliminary in vitro antitumor evaluation of HN-5 human carcinoma cell. | pt_BR |
dc.type | Artigo publicado em periodico | pt_BR |
dc.identifier.uri2 | https://www.degruyter.com/view/j/mgmc.2009.32.5/mgmc.2009.32.5.235/mgmc.2009.32.5.235.xml | pt_BR |
dc.identifier.doi | https://doi.org/10.1515/MGMC.2009.32.5.235 | - |
Aparece nas coleções: | DEQUI - Artigos publicados em periódicos |
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ARTIGO_SpectroscopicInvestigationOrganotin.pdf Restricted Access | 858,2 kB | Adobe PDF | Visualizar/Abrir |
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